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QC Testing

Labcorp's global analytical capabilities span the drug development life cycle, from initial discovery and early phase characterization work through to validations and routine quality control (QC) release and stability testing to support clinical trials and commercial release. We collaborate with you to provide a pragmatic, risk-assessed approach to meet project milestones efficiently and effectively at each stage of the drug development continuum.
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Our QC testing services 

We have successfully completed numerous global regulatory audits and offer a wide range of both non-cGMP and cGMP CMC biopharmaceutical services to support your analytical control strategy.

Validation

Before an analytical method can be used in a cGMP setting, it is necessary to show it is fit for purpose

Validation Services
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Release

A crucial component of the cGMP manufacture is the QC release testing of each batch

Release Services
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Stability

Stability assessment is another crucial component of QC testing required to support successful drug development

Stability Services
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Quality management

At Labcorp, we continuously strive to be a trusted, objective global drug development laboratory partner

Quality Management Services
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Scientific staff training

At Labcorp, we invest in our scientific staff training to enable the best outcomes for our clients

Scientific Staff Training Services
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